abnormal respiratory motile cilium physiology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any functional anomaly of the respiratory motile cilia. (Human Phenotype Ontology, HP_0012261)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012261
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Genes

19 genes associated with the abnormal respiratory motile cilium physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARMC4 armadillo repeat containing 4
C21ORF59 chromosome 21 open reading frame 59
CCDC103 coiled-coil domain containing 103
CCDC114 coiled-coil domain containing 114
CCDC39 coiled-coil domain containing 39
CCDC65 coiled-coil domain containing 65
DNAAF3 dynein, axonemal, assembly factor 3
DNAAF5 dynein, axonemal, assembly factor 5
DNAH11 dynein, axonemal, heavy chain 11
DNAI1 dynein, axonemal, intermediate chain 1
DNAL1 dynein, axonemal, light chain 1
DYX1C1 dyslexia susceptibility 1 candidate 1
HYDIN HYDIN, axonemal central pair apparatus protein
LRRC6 leucine rich repeat containing 6
NME8 NME/NM23 family member 8
RSPH4A radial spoke head 4 homolog A (Chlamydomonas)
RSPH9 radial spoke head 9 homolog (Chlamydomonas)
SPAG1 sperm associated antigen 1
ZMYND10 zinc finger, MYND-type containing 10